Variant #0000858662 (NC_000002.11:g.71825884G>T, NC_000002.11(NM_003494.3):c.3702+9G>T (DYSF))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.71825884G>T |
DNA change (hg38) |
- |
Published as |
DYSF(NM_001130455.1):c.3705+9G>T (p.(=)), DYSF(NM_001130981.1):c.3753+9G>T, DYSF(NM_001130981.2):c.3753+9G>T |
ISCN |
- |
DB-ID |
DYSF_000488 See all 6 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00058 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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